Evidence map›Paper›PMID 41692902›Full record

ArticleScientific reports2026

Construction of a nomogram prediction model for individualized prediction of vertebral compression fracture risk in postmenopausal osteoporosis population.

Jv Chen, Bo Wei, Jie Cai, Hao Lin, Chengshuo Huang

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Jv Chen *Department of Pharmacy, Affiliated Hospital of Guangdong Medical University, Zhanjiang City, 524000, China.
Bo Wei *Department of Orthopedic Center, Affiliated Hospital of Guangdong Medical University, No. 57 Renmin Avenue South, Xiashan District, Zhanjiang City, 524000, Guangdong Province, China.
Jie CaiDepartment of Pharmacy, Affiliated Hospital of Guangdong Medical University, Zhanjiang City, 524000, China.
Hao Lin *Department of Orthopedic Center, Affiliated Hospital of Guangdong Medical University, No. 57 Renmin Avenue South, Xiashan District, Zhanjiang City, 524000, Guangdong Province, China. Puningworker@163.com.
Chengshuo Huang *Department of Orthopedic Center, Affiliated Hospital of Guangdong Medical University, No. 57 Renmin Avenue South, Xiashan District, Zhanjiang City, 524000, Guangdong Province, China. huangkkjh8@sina.com.

Funding

2024 Guangdong Medical University Clinical+Basic Technology Innovation Special Plan GDMULCJC2024030
6 · The paper itself

Abstract

To construct a nomogram risk prediction model for osteoporotic vertebral compression fracture (OVCF) in postmenopausal osteoporosis (POP). A retrospective study was conducted on 326 POP patients from July 2023 to November 2024. The patients were randomly included into a training cohort of 228 cases and a validation cohort of 98 cases based on a 7:3 ratio; The training queue was assigned into a fracture group of 82 cases and a non fracture group of 146 cases. Risk factors were screened based on multiple logistic regression analysis. R software was used to construct nomogram prediction models. ROC curve, calibration curve, and clinical decision curve were performed to evaluate model discrimination, calibration, and practicality. For the non fracture group, the fracture group showed manifest increases in age, physical exercise time < 1 h/d, gastrointestinal diseases, uric acid, and type I collagen carboxy terminal peptide (β-CTX), and manifest decreases in bone mineral density (BMD) (T value), hemoglobin (Hb), and 5-hydroxyvitamin D [25-(OH)D] (P < 0.05). Increase in age, decrease in BMD (T value), physical exercise time < 1 h/d, presence of gastrointestinal diseases, increase in uric acid, increase in β-CTX, and decrease in 25-(OH)D were independent risk factors for OVCF in POP (P < 0.05). The calibration curves of the training queue and validation queue indicated a high degree of agreement between the predicted results of the model and the actual results, Hosmer-Lemeshow χ

Indexed as

Fractures, CompressionNomogramsOsteoporosis, PostmenopausalOsteoporotic FracturesSpinal FracturesAgedBone DensityFemaleHumansMiddle AgedPrediction AlgorithmsRetrospective StudiesRisk AssessmentRisk FactorsROC CurveForecastInfluencing factorsNomogramPostmenopausal osteoporosisVertebral compression fracture

Identifiers

PMID41692902
PMCPMC12996563

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.